The Alzheimer’s Registry
In our data-driven age, the emerging Alzheimer’s disease registry — a system that could collect and share biomarker, genetic, and clinical data from people at risk or with early-stage Alzheimer’s — sits at the intersection of societal benefits and individual rights. Photo by KOBU Agency on Unsplash The Registry Promoters claim such registries would generate effective therapies, improve public health planning, and reduce [...]